3
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: not found
      • Article: not found

      Hierarchical self-assembly of chiral fibres from achiral particles

      1 , 2 , 1
      Interface Focus
      The Royal Society

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          We investigate, by molecular dynamics simulation, the behaviour of discotic particles in a solvent of Lennard-Jones spheres. When chromonic disc-sphere interactions are imposed on these systems, three regimes of self-assembly are observed. At moderate temperatures, numerous short threads of discs develop, but these threads remain isolated from one another. Quenching to low temperatures, alternatively, causes all of the discs to floc into a single extended aggregate which typically comprises several distinct sections and contains numerous packing defects. For a narrow temperature range between these regimes, however, defect-free chiral fibres are found to freely self-assemble. The spontaneous chirality of these fibres results from frustration between the hexagonal packing and interdigitation of neighbouring threads, the pitch being set by the particle shape. This demonstration of aggregate-wide chirality emerging owing to packing alone is pertinent to many biological and synthetic hierarchically self-assembling systems.

          Related collections

          Most cited references26

          • Record: found
          • Abstract: not found
          • Article: not found

          Dendron-mediated self-assembly, disassembly, and self-organization of complex systems.

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Dynamic order-disorder in atomistic models of structural glass formers.

            The glass transition is the freezing of a liquid into a solid state without evident structural order. Although glassy materials are well characterized experimentally, the existence of a phase transition into the glass state remains controversial. Here, we present numerical evidence for the existence of a novel first-order dynamical phase transition in atomistic models of structural glass formers. In contrast to equilibrium phase transitions, which occur in configuration space, this transition occurs in trajectory space, and it is controlled by variables that drive the system out of equilibrium. Coexistence is established between an ergodic phase with finite relaxation time and a nonergodic phase of immobile molecular configurations. Thus, we connect the glass transition to a true phase transition, offering the possibility of a unified picture of glassy phenomena.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Supracolloidal reaction kinetics of Janus spheres.

              Clusters in the form of aggregates of a small number of elemental units display structural, thermodynamic, and dynamic properties different from those of bulk materials. We studied the kinetic pathways of self-assembly of "Janus spheres" with hemispherical hydrophobic attraction and found key differences from those characteristic of molecular amphiphiles. Experimental visualization combined with theory and molecular dynamics simulation shows that small, kinetically favored isomers fuse, before they equilibrate, into fibrillar triple helices with at most six nearest neighbors per particle. The time scales of colloidal rearrangement combined with the directional interactions resulting from Janus geometry make this a prototypical system to elucidate, on a mechanistic level and with single-particle kinetic resolution, how chemical anisotropy and reaction kinetics coordinate to generate highly ordered structures.
                Bookmark

                Author and article information

                Journal
                Interface Focus
                Interface Focus
                The Royal Society
                2042-8898
                2042-8901
                February 2012
                October 06 2012
                March 28 2012
                October 06 2012
                : 2
                : 5
                : 651-657
                Affiliations
                [1 ]Materials and Engineering Research Institute, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, UK
                [2 ]Unilever Discover, Colworth Laboratories, Bedfordshire MK44 1LQ, UK
                Article
                10.1098/rsfs.2011.0104
                3438579
                24098850
                6efb68fd-efec-42b7-b139-fd072b023f1e
                © 2012
                History

                Comments

                Comment on this article